Myoclonus-dystonia syndrome: Clinical presentation, disease course, and genetic features in 11 families-Reference-Cited by-同舟云学术

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Myoclonus-dystonia syndrome: Clinical presentation, disease course, and genetic features in 11 families

Published:2007-09-12 Issue:1 Volume:23 Page:28-34
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov. Disord.

Author:

Nardocci Nardo,Zorzi Giovanna,Barzaghi Chiara,Zibordi Federica,Ciano Claudia,Ghezzi Daniele,Garavaglia Barbara

Funder

ALDEI Foundation

National Ministry of Health

Paolo Zorzi Association

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/mds.21715/fullpdf

Reference21 articles.

1. Inherited myoclonus dystonia;Asmus;Adv Neurol,2004

2. Mutations in the gene encoding ϵ-sarcoglycan cause myoclonus-dystonia syndrome;Zimprich;Nat Genet,2001

3. Epsilon sarcoglycan mutations found in combination with other dystonia gene mutations;Klein;Ann Neurol,2002

4. Autosomal dominant GTP-CH deficiency presenting as a Dopa-responsive myoclonus dystonia syndrome;Leuzzi;Neurology,2002

5. Analysis of the epsilon sarcoglycan gene in familial and sporadic myoclonus-dystonia: evidence for genetic heterogeneity;Valente;Mov Disord,2003

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1. The effect of valproate on dystonic movement in a moyamoya patient: A case report;Neurology Asia;2024-03

2. Clinical and genetic profile of patients with dystonia: An experience from a tertiary neurology center from India;Parkinsonism & Related Disorders;2024-03

3. Dystonia Responding to Levodopa in A Child with Myoclonus‐Dystonia;Movement Disorders Clinical Practice;2023-03-07

4. Early recognition of SGCE ‐myoclonus–dystonia in children;Developmental Medicine & Child Neurology;2022-06-20

5. A Clinical Approach to the Patients with Combination of Dystonia and Myoclonus;Annals of Movement Disorders;2022-05

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